US4397934A - Developer compositions containing quaternized vinylpyridine polymers, and copolymers - Google Patents
Developer compositions containing quaternized vinylpyridine polymers, and copolymers Download PDFInfo
- Publication number
- US4397934A US4397934A US06/336,242 US33624281A US4397934A US 4397934 A US4397934 A US 4397934A US 33624281 A US33624281 A US 33624281A US 4397934 A US4397934 A US 4397934A
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- US
- United States
- Prior art keywords
- accordance
- percent
- partially quaternized
- poly
- vinylpyridine
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims abstract description 51
- 229920000642 polymer Polymers 0.000 title claims abstract description 23
- 229920001577 copolymer Polymers 0.000 title claims abstract description 22
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 title description 5
- 239000002245 particle Substances 0.000 claims abstract description 57
- 239000011347 resin Substances 0.000 claims abstract description 35
- 229920005989 resin Polymers 0.000 claims abstract description 35
- 239000000463 material Substances 0.000 claims abstract description 23
- 239000000049 pigment Substances 0.000 claims abstract description 22
- WDRZVZVXHZNSFG-UHFFFAOYSA-N 1-ethenylpyridin-1-ium Chemical compound C=C[N+]1=CC=CC=C1 WDRZVZVXHZNSFG-UHFFFAOYSA-N 0.000 claims abstract description 16
- 238000003384 imaging method Methods 0.000 claims abstract description 15
- 230000002708 enhancing effect Effects 0.000 claims abstract description 13
- 150000001450 anions Chemical class 0.000 claims abstract description 8
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims abstract description 7
- 150000002367 halogens Chemical class 0.000 claims abstract description 6
- JEVCWSUVFOYBFI-UHFFFAOYSA-N cyanyl Chemical compound N#[C] JEVCWSUVFOYBFI-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052739 hydrogen Chemical group 0.000 claims abstract description 5
- 239000001257 hydrogen Chemical group 0.000 claims abstract description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 5
- 150000002431 hydrogen Chemical group 0.000 claims abstract 3
- 125000000217 alkyl group Chemical group 0.000 claims abstract 2
- -1 halogen anion Chemical class 0.000 claims description 50
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 47
- 238000000034 method Methods 0.000 claims description 24
- MPPPKRYCTPRNTB-UHFFFAOYSA-N 1-bromobutane Chemical compound CCCCBr MPPPKRYCTPRNTB-UHFFFAOYSA-N 0.000 claims description 21
- SOGAXMICEFXMKE-UHFFFAOYSA-N alpha-Methyl-n-butyl acrylate Natural products CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 claims description 10
- 239000006229 carbon black Substances 0.000 claims description 10
- 229920000075 poly(4-vinylpyridine) Polymers 0.000 claims description 10
- KFDVPJUYSDEJTH-UHFFFAOYSA-N 4-ethenylpyridine Chemical compound C=CC1=CC=NC=C1 KFDVPJUYSDEJTH-UHFFFAOYSA-N 0.000 claims description 9
- 229920000885 poly(2-vinylpyridine) Polymers 0.000 claims description 8
- NAMYKGVDVNBCFQ-UHFFFAOYSA-N 2-bromopropane Chemical compound CC(C)Br NAMYKGVDVNBCFQ-UHFFFAOYSA-N 0.000 claims description 6
- 229910000831 Steel Inorganic materials 0.000 claims description 6
- 239000010959 steel Substances 0.000 claims description 6
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical compound FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 3
- 229910002651 NO3 Inorganic materials 0.000 claims description 3
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 3
- 229910019142 PO4 Inorganic materials 0.000 claims description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 3
- 150000004820 halides Chemical class 0.000 claims description 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 3
- 239000010452 phosphate Substances 0.000 claims description 3
- 239000000758 substrate Substances 0.000 claims description 3
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 3
- 229920001774 Perfluoroether Polymers 0.000 claims 3
- 229920002313 fluoropolymer Polymers 0.000 claims 3
- 239000004811 fluoropolymer Substances 0.000 claims 3
- 150000001721 carbon Chemical group 0.000 claims 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 101150108015 STR6 gene Proteins 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 238000011161 development Methods 0.000 abstract description 6
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 abstract 1
- 101150035983 str1 gene Proteins 0.000 abstract 1
- 229920002554 vinyl polymer Polymers 0.000 description 8
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 6
- 239000000969 carrier Substances 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 108091008695 photoreceptors Proteins 0.000 description 6
- 239000003086 colorant Substances 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 229920006026 co-polymeric resin Polymers 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 229910052759 nickel Inorganic materials 0.000 description 3
- USZXSOMZYDRNPS-UHFFFAOYSA-N 2-benzylidenecarbazol-1-amine Chemical compound NC1=C2N=C3C=CC=CC3=C2C=CC1=CC1=CC=CC=C1 USZXSOMZYDRNPS-UHFFFAOYSA-N 0.000 description 2
- ZGHFDIIVVIFNPS-UHFFFAOYSA-N 3-Methyl-3-buten-2-one Chemical compound CC(=C)C(C)=O ZGHFDIIVVIFNPS-UHFFFAOYSA-N 0.000 description 2
- GXHFAFFBRFVGLX-UHFFFAOYSA-N 4-(4-aminophenyl)-2,3-bis(3-methylphenyl)aniline Chemical compound CC1=CC=CC(C=2C(=C(C=3C=CC(N)=CC=3)C=CC=2N)C=2C=C(C)C=CC=2)=C1 GXHFAFFBRFVGLX-UHFFFAOYSA-N 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- 238000012644 addition polymerization Methods 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 239000012876 carrier material Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 150000002009 diols Chemical class 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 229920001519 homopolymer Polymers 0.000 description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- YRZZLAGRKZIJJI-UHFFFAOYSA-N oxyvanadium phthalocyanine Chemical compound [V+2]=O.C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 YRZZLAGRKZIJJI-UHFFFAOYSA-N 0.000 description 2
- 229920003227 poly(N-vinyl carbazole) Polymers 0.000 description 2
- 229920005668 polycarbonate resin Polymers 0.000 description 2
- 239000004431 polycarbonate resin Substances 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- FYADHXFMURLYQI-UHFFFAOYSA-N 1,2,4-triazine Chemical compound C1=CN=NC=N1 FYADHXFMURLYQI-UHFFFAOYSA-N 0.000 description 1
- KTZVZZJJVJQZHV-UHFFFAOYSA-N 1-chloro-4-ethenylbenzene Chemical compound ClC1=CC=C(C=C)C=C1 KTZVZZJJVJQZHV-UHFFFAOYSA-N 0.000 description 1
- CNDHHGUSRIZDSL-UHFFFAOYSA-N 1-chlorooctane Chemical compound CCCCCCCCCl CNDHHGUSRIZDSL-UHFFFAOYSA-N 0.000 description 1
- OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 description 1
- RCSKFKICHQAKEZ-UHFFFAOYSA-N 1-ethenylindole Chemical compound C1=CC=C2N(C=C)C=CC2=C1 RCSKFKICHQAKEZ-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- QAHMKHHCOXNIHO-UHFFFAOYSA-N 2,4-diphenylquinazoline Chemical compound C1=CC=CC=C1C1=NC(C=2C=CC=CC=2)=C(C=CC=C2)C2=N1 QAHMKHHCOXNIHO-UHFFFAOYSA-N 0.000 description 1
- XKZQKPRCPNGNFR-UHFFFAOYSA-N 2-(3-hydroxyphenyl)phenol Chemical compound OC1=CC=CC(C=2C(=CC=CC=2)O)=C1 XKZQKPRCPNGNFR-UHFFFAOYSA-N 0.000 description 1
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 description 1
- WHBAYNMEIXUTJV-UHFFFAOYSA-N 2-chloroethyl prop-2-enoate Chemical compound ClCCOC(=O)C=C WHBAYNMEIXUTJV-UHFFFAOYSA-N 0.000 description 1
- CFVWNXQPGQOHRJ-UHFFFAOYSA-N 2-methylpropyl prop-2-enoate Chemical compound CC(C)COC(=O)C=C CFVWNXQPGQOHRJ-UHFFFAOYSA-N 0.000 description 1
- WUMNREMXKHAYJQ-UHFFFAOYSA-N 5-methyl-2,3-diphenyl-1,3-dihydropyrazole Chemical compound N1C(C)=CC(C=2C=CC=CC=2)N1C1=CC=CC=C1 WUMNREMXKHAYJQ-UHFFFAOYSA-N 0.000 description 1
- LRSYZHFYNDZXMU-UHFFFAOYSA-N 9h-carbazol-3-amine Chemical compound C1=CC=C2C3=CC(N)=CC=C3NC2=C1 LRSYZHFYNDZXMU-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000004593 Epoxy Substances 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 229920006370 Kynar Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- 239000002033 PVDF binder Substances 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 238000010539 anionic addition polymerization reaction Methods 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 235000021028 berry Nutrition 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- DFYKHEXCUQCPEB-UHFFFAOYSA-N butyl 2-methylprop-2-enoate;styrene Chemical compound C=CC1=CC=CC=C1.CCCCOC(=O)C(C)=C DFYKHEXCUQCPEB-UHFFFAOYSA-N 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 238000010538 cationic polymerization reaction Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 238000012674 dispersion polymerization Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 235000019441 ethanol Nutrition 0.000 description 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000000816 ethylene group Chemical class [H]C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical class O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical class C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- PBZROIMXDZTJDF-UHFFFAOYSA-N hepta-1,6-dien-4-one Chemical compound C=CCC(=O)CC=C PBZROIMXDZTJDF-UHFFFAOYSA-N 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- AWJZTPWDQYFQPQ-UHFFFAOYSA-N methyl 2-chloroprop-2-enoate Chemical compound COC(=O)C(Cl)=C AWJZTPWDQYFQPQ-UHFFFAOYSA-N 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- XLGSXVUJWBCURQ-UHFFFAOYSA-N n-(4-bromophenyl)-1-(2-nitrophenyl)methanimine Chemical compound [O-][N+](=O)C1=CC=CC=C1C=NC1=CC=C(Br)C=C1 XLGSXVUJWBCURQ-UHFFFAOYSA-N 0.000 description 1
- DWXAPYADWDBIII-UHFFFAOYSA-N n-[[4-(dimethylamino)phenyl]methylideneamino]benzamide Chemical compound C1=CC(N(C)C)=CC=C1C=NNC(=O)C1=CC=CC=C1 DWXAPYADWDBIII-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- HILCQVNWWOARMT-UHFFFAOYSA-N non-1-en-3-one Chemical compound CCCCCCC(=O)C=C HILCQVNWWOARMT-UHFFFAOYSA-N 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ANISOHQJBAQUQP-UHFFFAOYSA-N octyl prop-2-enoate Chemical compound CCCCCCCCOC(=O)C=C ANISOHQJBAQUQP-UHFFFAOYSA-N 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical class C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- WRAQQYDMVSCOTE-UHFFFAOYSA-N phenyl prop-2-enoate Chemical compound C=CC(=O)OC1=CC=CC=C1 WRAQQYDMVSCOTE-UHFFFAOYSA-N 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000647 polyepoxide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920005749 polyurethane resin Polymers 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 229920000131 polyvinylidene Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 229910052711 selenium Inorganic materials 0.000 description 1
- 239000011669 selenium Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 229920005992 thermoplastic resin Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- FUSUHKVFWTUUBE-UHFFFAOYSA-N vinyl methyl ketone Natural products CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 1
- XOSXWYQMOYSSKB-LDKJGXKFSA-L water blue Chemical compound CC1=CC(/C(\C(C=C2)=CC=C2NC(C=C2)=CC=C2S([O-])(=O)=O)=C(\C=C2)/C=C/C\2=N\C(C=C2)=CC=C2S([O-])(=O)=O)=CC(S(O)(=O)=O)=C1N.[Na+].[Na+] XOSXWYQMOYSSKB-LDKJGXKFSA-L 0.000 description 1
- 229910052845 zircon Inorganic materials 0.000 description 1
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 1
- 229910000859 α-Fe Inorganic materials 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/10—Developers with toner particles characterised by carrier particles
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G9/00—Developers
- G03G9/08—Developers with toner particles
- G03G9/10—Developers with toner particles characterised by carrier particles
- G03G9/113—Developers with toner particles characterised by carrier particles having coatings applied thereto
- G03G9/1132—Macromolecular components of coatings
- G03G9/1133—Macromolecular components of coatings obtained by reactions only involving carbon-to-carbon unsaturated bonds
- G03G9/1134—Macromolecular components of coatings obtained by reactions only involving carbon-to-carbon unsaturated bonds containing fluorine atoms
Definitions
- This invention is generally directed to developer compositions which can be utilized for the development of images in electrostatographic imaging systems. More specifically, the present invention is directed to developer compositions containing quaternized vinyl pyridine polymers, and copolymers, as charge enhancing components.
- the quaternized vinyl pyridine components of the present invention impart a positive charge to the toner particles, enabling such particles to be utilized for the development of negatively charged electrostatic latent images.
- the electrostatographic process and more specifically, the xerographic process is well known as documented in several prior art references. These processes involve the application of toner particles to the electrostatic latent image, for the purpose of causing development of such images. In some instances it may be desirable to produce a negative copy from a positive original, or a positive copy from a negative original, known as image reversal.
- image reversal can be accomplished by applying to the image a developer composition, containing toner particles and carrier particles, wherein the toner particles are repelled by the charged areas of the image, but adhere to the discharged areas.
- toner particles possessing positive charges are very useful and effective in electrostatographic reversal systems, especially those employing organic photoreceptors, which in many instances are charged negatively.
- Reversal developers which are comprised of electroscopic materials coated with finely divided colloidal silica are described for example, in U.S. Pat. No. 2,986,521.
- toners and developers have a tendency over a period of time to lose their positive charge.
- the charge control additives employed are incompatible with the thermoplastic toner resin, thus causing difficulties in obtaining a uniform dispersion of such additives in the toner resin.
- charge control agents are not compatible with the toner resin, they adversely affect the electrical properties of the resin. Additionally, primarily because of their low molecular weight, such charge control agents have been known to leach out of the toner composition, and contaminate the carrier surface.
- Another feature of this invention is the provision of a developer composition which contains positive charged toner particles, and certain charge enhancing components.
- a further feature of the present invention is the provision of partially quaternized vinyl pyridinium polymers, and copolymers, as charge enhancing components.
- Another feature of the present invention is to provide developer compositions useful for causing the development of negative electrostatic images, which compositions will transfer effectively, electrostatically to plain bond paper without causing blurring, or otherwise adversely affecting the quality of the resulting image.
- developer compositions comprised of resin particles, pigment particles, carrier particles, and a partially quaternized vinyl pyridinium polymer, including copolymers, selected from the group consisting of those materials as represented by the following formulas: ##STR2## wherein R is an alkyl radical, A is an anion, B is an alkyl radical or hydrogen, S is an acrylate, phenyl, halogen, or cyano radical, x, y, u, v, and w represent weight fraction numbers, (weight of monomer divided by total weight of polymer) subject to the provision that x+y is equal to 1, and the sum of u+v+w is equal to 1.
- the symbol x can thus be a number of less than 1, for example x can be a number of from about 0.1 to about 0.9.
- x is the number 0.9
- y is the number 0.1.
- the symbols u, v, and w can be numbers of from 0.1 to about 0.9, subject to the provision that the sum of these numbers is equal to 1.
- alkyl radicals include those containing from 1 to about 20 carbon atoms, and preferably those containing from 1 to about 6 carbon atoms, such as methyl, ethyl, propyl, butyl, pentyl, octyl, nonyl, decyl, myristyl, cetyl, olely, and the like, with methyl, propyl, and butyl being preferred.
- Illustrative examples of the anion A include halides, such as chloride, fluoride, bromide or iodide, sulfate, sulfonate, borate, nitrate and phosphate, with the anions chloride and bromide being preferred.
- halides such as chloride, fluoride, bromide or iodide, sulfate, sulfonate, borate, nitrate and phosphate, with the anions chloride and bromide being preferred.
- Illustrative examples of specific partially quaternized vinyl pyridinium polymers and copolymers embraced within the present invention include for example poly(2-vinyl pyridine) partially quaternized with butyl bromide, poly(4-vinyl pyridine) partially quaternized with butyl bromide, poly(2-vinyl pyridine/styrene) partially quaternized with isopropyl bromide, poly(4-vinyl pyridine/styrene) partially quaternized with butyl bromide, poly(4-vinyl pyridine) partially quaternaized with octyl chloride, poly(styrene/n-butyl methacryalte/4-vinyl pyridine), partially quaternized with n-butyl bromide, and the like.
- Poly(4-vinyl pyridine) partially quaternized with n-butyl bromide can be represented by the following: ##STR3## while the copolymers of 4-vinyl pyridine and styrene partially quaternized with n-butyl bromide can be represented by the following: ##STR4## wherein the sum of x plus y is equal to 1, and the sum of u plus v, plus w is equal to 1.
- the partially quaternized vinyl pyridinium polymers, and copolymers, of the present invention are added to the toner particles in an amount that does not adversely affect the properties of such particles, and that results in a toner that is charged positively, in comparison to the carrier.
- the amount of quaternized vinyl pyridinium material present in the developer composition can vary from about 0.1 weight percent to about 98 weight percent, and preferably from about 1 weight percent to about 10 weight percent.
- the partially quaternized vinyl pyridinium materials can be blended into the developer mixture, or coated on a pigment, such as carbon black, which is used as a colorant in the developing composition.
- developing composition is meant a composition comprised of toner particles, toner resin plus pigment, and carrier particles.
- Suitable resins may be employed in the toner composition of the present invention, including polyamides, epoxies, polyurethanes, vinyl resins and polyesters, especially those prepared from dicarboxylic acids and diols comprising diphenols.
- Any suitable vinyl resin may be employed in the toners of the present system, including homopolymers or copolymers of two or more vinyl monomers.
- vinyl monomeric units include: styrene, p-chlorostyrene, vinyl naphthalene, ethylenically unsaturated monoolefins such as ethylene, propylene, butylene, isobutylene and the like; vinyl halides such as vinyl chloride, vinyl bromide, vinyl fluoride, vinyl esters such as vinyl acetate, vinyl propionate, vinyl benzoate, vinyl butyrate and the like; esters of aliphamethylene aliphatic monocarboxylic acids such as methyl acrylate, ethyl acrylate, n-butylacrylate, isobutyl acrylate, dodecyl acrylate, n-octyl acrylate, 2-chloroethyl acrylate, phenyl acrylate, methylalpha-chloroacrylate, methyl methacrylate, ethyl methacrylate, butyl methacrylate and the like;
- toner resins containing a relatively high percentage of styrene are preferred.
- the styrene resin employed may be a homopolymer of styrene or styrene homologs of copolymers of styrene with other monomeric groups. Any of the above typical monomeric units may be copolymerized with styrene by addition polymerization.
- Styrene resins may also be formed by the polymerization of mixtures of two or more unsaturated monomeric materials with a styrene monomer.
- the addition polymerization technique employed embraces known polymerization techniques such as free radical, anionic, and cationic polymerization processes.
- any of these vinyl resins may be blended with one or more resins if desired, preferably other vinyl resins, which insure good triboelectric properties and uniform resistance against physical degradation.
- nonvinyl type thermoplastic resins may also be employed including resin modified phenolformaldehyde resins, oil modified epoxy resins, polyurethane resins, cellulosic resins, polyether resins, and mixtures thereof.
- esterification products of a dicarboxylic acid, and a diol comprising a diphenol may be used as a preferred resin material for the toner composition of the present invention, as illustrated in U.S. Pat. No. 3,655,374, the disclosure of which is totally incorporated herein by reference.
- any suitable pigment or dye may be employed as the colorant for the toner particles, such materials being well known and including for example, carbon black, nigrosine dye, aniline blue, calco oil blue, chrome yellow, ultramarine blue, phthalocyanine blue and mixtures thereof.
- the pigment or dye should be present in the toner in sufficient quantity to render it highly colored, so that the toner will form a clearly visible image on the recording member.
- the toner may comprise a black pigment, such as carbon black.
- the pigment is employed in amounts of from about 2 percent to about 20 percent by weight, based on the total weight of the toner particles, however, if the colorant employed is a dye, substantially smaller quantities may be used.
- the toner resin is present in an amount so that the total of all ingredients used equal about 100 percent, thus when 5 percent by weight of the partially quaternized vinyl pyridine polymer is present, and 10 percent by weight of pigment or colorant such as carbon black, about 85 percent by weight of resin material is present.
- carrier particles useful in the present invention include those carrier particles which are capable of triboelectrically obtaining a charge of opposite polarity to that of the toner particles.
- the carrier particles can be selected so that the toner particles acquire a charge of a positive polarity, and include materials such as potassium chlorate, granular zircon, granular silicon, methylmethacrylate, glass, steel, nickel, iron ferrites, silicon dioxide and the like, with metallic carriers especially magnetic carriers being preferred.
- the carriers can be used with or without a coating.
- the coatings generally contain polyvinyl fluoride resins, but other resins especially those which charge negatively, such as polystyrene, halogen containing ethylenes and the like can be used.
- polystyrene polystyrene resin
- halogen containing ethylenes and the like many of the typical carriers that can be used are described in U.S. Pat. Nos. 2,618,441; 2,638,522; 3,618,522; 3,591,503; 3,533,835; and 3,526,533.
- nickel berry carriers as described in U.S. Pat. Nos. 3,847,604 and 3,767,598 can be employed, these carriers being nodular carrier beads of nickel characterized by surface of reoccurring recesses and protrusions providing particles with a relatively large external area.
- the diameter of the coated carrier particle is from about 50 to about 1,000 microns, thus allowing the carrier to possess sufficient density and inertia to avoid adherence to the electrostatic images during the development
- the carrier may be employed with the toner composition in any suitable combination, however, best results are obtained when about 0.5 parts to about 10 parts of toner, to 100 to 200 parts by weight of carrier, and preferably about 1 part to 5 parts of toner, to 100 parts by weight of carrier.
- Developer compositions of the present invention may be used to develop electrostatic latent images on various suitable electrostatic surfaces capable of retaining charge including conventional photoconductors, however, the toners of the present invention are best utilized in systems wherein a negative charge resides on the photoreceptor, and this usually occurs with organic photoreceptors.
- photoreceptors examples include polyvinyl carbazole, 4-dimethylaminobenzylidene, benzhydrazide; 2-benzylidene-amino-carbazole, 4-dimethylamino-benzylidene, benzyhydrazide; 2-benzylidene-aminocarbazole, polyvinylcarbazole; (2-nitro-benzylidene)-p-bromoaniline; 2,4-diphenyl-quinazoline; 1,2,4-triazine; 1,5-diphenyl- 3-methyl pyrazoline 2-(4'-dimethyl-amino phenyl)-benzoxazole; 3-aminocarbazole; polyvinylcarbazole-tritrofluorenone charge transfer complex; phthalocyanines, overcoated photoreceptors containing charge transport and charge generating layers, and the like.
- charge generating layers include vanadyl phthalocyanine, and trigonal selenium
- charge transport layers include certain diamines, such as N,N'-diphenyl-N-N' bis(3-methylphenyl)-[1,1'-biphenyl]-4,4'-diamine, dispersed in a polycarbonate resin, reference U.S. Pat. No. 4,251,612, the disclosure of which is totally incorporated herein by reference.
- Numerous methods may be utilized to produce the toner composition of the present invention, one method involving melt blending the resin and the pigment with the partially quaternized vinyl pyridinium material, followed by mechanical attrition.
- Other methods include those well known in the art such as spray drying, melt dispersion, and dispersion polymerization.
- a solvent dispersion of a resin pigment and a partially quaternized vinyl pyridinium polymer and copolymer are spray dryed under controlled conditions, thereby resulting in the desired product.
- a composition prepared in this manner results in a positively charged toner in relationship to the carrier materials, and these materials exhibit the improved properties as mentioned herein.
- the present invention is directed to a method of imaging comprising forming a negative electrostatic latent image on a photoresponsive device, contacting the image with a developer composition, comprised of resin particles, pigment particles, carrier particles, and a charge enhancing component comprised of partially quaternized vinylpyridinium polymers, including copolymers selected from the group consisting of those materials of the following formula: ##STR5## followed by transferring the developed image to a suitable substrate, and fixing the image thereto, wherein R is an alkyl radical, A is an anion, B is an alkyl radical or hydrogen, S is an acrylate, phenyl, halogen, or cyano radical, x, y, u, v, and w represent weight fraction numbers, (weight of monomer divided by total weight of polymer) subject to the provision that x+y is equal to 1, and the sum of u+v+w is equal to 1.
- a developer composition comprised of resin particles, pigment particles, carrier particles, and a charge enhancing component comprised
- x can thus be a number of less than 1, for example, x can be a number of from about 0.1 to about 0.9.
- y is the number 0.1.
- the symbols u, v, and w can be numbers of from 0.1 to about 0.9, subject to the provision that the sum of these numbers is equal to 1.
- the above developer was utilized in a xerographic fixture, employing a negatively charged photoreceptor device, containing a vanadyl phthalocyanine photogenerating layer, and a transport layer of N-N'-diphenyl-N-N' bis(3-methylphenyl)-[1,1'-biphenyl]-4,4'-diamine dispersed in a polycarbonate resin, and prints of excellent quality and superior resolution were obtained. Also the prints had high solid area density and low background density.
- Toner tribos against the carrier described in Example II were as follows:
- Example II The developer compositions of Examples II and III were utilized in the xerographic device of Example I, and substantially similar results were obtained.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Developing Agents For Electrophotography (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
Description
______________________________________
Toner Tribo uc/g
Time (Microcoulombs per gram)
______________________________________
10 min. +42
1 hour +42
4 hours +39
24 hours +26
______________________________________
______________________________________
Toner Tribo, uc/g
Time (Microcoulombs per gram)
______________________________________
10 min. +36
1 hour +26
4 hours +20
24 hours +14
______________________________________
______________________________________
Toner Tribo, uc/g
Time (Microcoulombs per gram)
______________________________________
10 min. +40
1 hour +35
4 hours +27
24 hours +17
______________________________________
Claims (20)
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/336,242 US4397934A (en) | 1981-12-31 | 1981-12-31 | Developer compositions containing quaternized vinylpyridine polymers, and copolymers |
| GB08236121A GB2114763B (en) | 1981-12-31 | 1982-12-20 | Electrophotographic developer composition |
| JP57235103A JPS58120263A (en) | 1981-12-31 | 1982-12-24 | Developer composition containing 4-level vinylpyridine |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/336,242 US4397934A (en) | 1981-12-31 | 1981-12-31 | Developer compositions containing quaternized vinylpyridine polymers, and copolymers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4397934A true US4397934A (en) | 1983-08-09 |
Family
ID=23315193
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US06/336,242 Expired - Fee Related US4397934A (en) | 1981-12-31 | 1981-12-31 | Developer compositions containing quaternized vinylpyridine polymers, and copolymers |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US4397934A (en) |
| JP (1) | JPS58120263A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0185509A1 (en) * | 1984-12-18 | 1986-06-25 | Xerox Corporation | Toner compositions |
| US4737434A (en) * | 1986-03-31 | 1988-04-12 | Xerox Corporation | Process for colored toners with selected triboelectric characteristics |
| US5187038A (en) * | 1990-09-19 | 1993-02-16 | Hoechst Aktiengesellschaft | Polymeric ammonium compounds as charge control agents |
| US20100173241A1 (en) * | 2007-05-29 | 2010-07-08 | Zeon Corporation | Positively-chargeable toner for developing electrostatic image |
| CN119662022A (en) * | 2024-12-25 | 2025-03-21 | 深圳市富恒新材料股份有限公司 | Conductive wear-resistant polyphenylene sulfide/polyketone composite material and preparation method thereof |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2761384B2 (en) * | 1987-12-01 | 1998-06-04 | 株式会社リコー | Electrostatic toner |
| US5385802A (en) * | 1990-10-08 | 1995-01-31 | Fuji Xerox Co., Ltd. | Process for producing toner |
| JP6387983B2 (en) * | 2016-02-23 | 2018-09-12 | 京セラドキュメントソリューションズ株式会社 | Toner for electrostatic latent image development |
Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3893935A (en) * | 1972-05-30 | 1975-07-08 | Eastman Kodak Co | Electrographic toner and developer composition |
| US3944493A (en) * | 1974-05-16 | 1976-03-16 | Eastman Kodak Company | Electrographic toner and developer composition |
| US3985664A (en) * | 1973-12-29 | 1976-10-12 | Kao Soap Co., Ltd. | Toner composition for use in electrophotography comprising novel polyester binder resin |
| US4079014A (en) * | 1976-07-21 | 1978-03-14 | Eastman Kodak Company | Electrographic toner and developer composition containing a 4-aza-1-azoniabicyclo(2.2.2) octane salt as a charge control agent |
| GB1536514A (en) | 1976-01-23 | 1978-12-20 | Oce Van Der Grinten Nv | Developer powder for electrostatic images and preparation of such powder |
| US4221856A (en) * | 1978-04-03 | 1980-09-09 | Xerox Corporation | Electrographic toner containing resin-compatible quaternary ammonium compound |
| US4224396A (en) * | 1978-03-02 | 1980-09-23 | Xerox Corporation | Magnetic toner materials containing quaternary ammonium polymers as charge control agents |
| US4298672A (en) * | 1978-06-01 | 1981-11-03 | Xerox Corporation | Toners containing alkyl pyridinium compounds and their hydrates |
| US4299898A (en) * | 1979-05-03 | 1981-11-10 | Xerox Corporation | Positively charged toners containing quaternary ammonium salts attached to acrylate polymers |
-
1981
- 1981-12-31 US US06/336,242 patent/US4397934A/en not_active Expired - Fee Related
-
1982
- 1982-12-24 JP JP57235103A patent/JPS58120263A/en active Pending
Patent Citations (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3893935A (en) * | 1972-05-30 | 1975-07-08 | Eastman Kodak Co | Electrographic toner and developer composition |
| US3985664A (en) * | 1973-12-29 | 1976-10-12 | Kao Soap Co., Ltd. | Toner composition for use in electrophotography comprising novel polyester binder resin |
| US3944493A (en) * | 1974-05-16 | 1976-03-16 | Eastman Kodak Company | Electrographic toner and developer composition |
| GB1536514A (en) | 1976-01-23 | 1978-12-20 | Oce Van Der Grinten Nv | Developer powder for electrostatic images and preparation of such powder |
| US4079014A (en) * | 1976-07-21 | 1978-03-14 | Eastman Kodak Company | Electrographic toner and developer composition containing a 4-aza-1-azoniabicyclo(2.2.2) octane salt as a charge control agent |
| US4224396A (en) * | 1978-03-02 | 1980-09-23 | Xerox Corporation | Magnetic toner materials containing quaternary ammonium polymers as charge control agents |
| US4221856A (en) * | 1978-04-03 | 1980-09-09 | Xerox Corporation | Electrographic toner containing resin-compatible quaternary ammonium compound |
| US4298672A (en) * | 1978-06-01 | 1981-11-03 | Xerox Corporation | Toners containing alkyl pyridinium compounds and their hydrates |
| US4299898A (en) * | 1979-05-03 | 1981-11-10 | Xerox Corporation | Positively charged toners containing quaternary ammonium salts attached to acrylate polymers |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0185509A1 (en) * | 1984-12-18 | 1986-06-25 | Xerox Corporation | Toner compositions |
| US4621039A (en) * | 1984-12-18 | 1986-11-04 | Xerox Corporation | Developer compositions with fast admixing characteristics |
| JPH0810357B2 (en) | 1984-12-18 | 1996-01-31 | ゼロツクス コーポレーシヨン | Improved toner composition |
| US4737434A (en) * | 1986-03-31 | 1988-04-12 | Xerox Corporation | Process for colored toners with selected triboelectric characteristics |
| US5187038A (en) * | 1990-09-19 | 1993-02-16 | Hoechst Aktiengesellschaft | Polymeric ammonium compounds as charge control agents |
| US20100173241A1 (en) * | 2007-05-29 | 2010-07-08 | Zeon Corporation | Positively-chargeable toner for developing electrostatic image |
| CN119662022A (en) * | 2024-12-25 | 2025-03-21 | 深圳市富恒新材料股份有限公司 | Conductive wear-resistant polyphenylene sulfide/polyketone composite material and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS58120263A (en) | 1983-07-18 |
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